Test ID: HPKM
Hereditary Pancreatitis, Known Mutation
Method Description 
Describes how the test is performed and provides a method-specific reference
DNA sequence analysis, using fluorescent Sanger dideoxy terminator chemistry and detection using capillary array electrophoresis, is used to test for the presence of a mutation in exons 2 and 3 of the cationic trypsinogen (PRSS1) gene. (Unpublished Mayo method)
Day(s) and Time(s) Test Performed Outlines the days and times the test is performed. This field reflects the day and time the sample must be in the testing laboratory to begin the testing process and includes any specimen preparation and processing time required before the test is performed. Some tests are listed as continuously performed, which means assays are performed several times during the day.
Wednesday; 10 a.m.
Analytic Time Defines the amount of time it takes the laboratory to setup and perform the test. This is defined in number of days. The shortest interval of time expressed is "same day/1 day," which means the results may be available the same day that the sample is received in the testing laboratory. One day means results are available 1 day after the sample is received in the laboratory.
10 days
Maximum Laboratory Time Defines the maximum time from specimen receipt at Mayo Medical Laboratories until the release of the test result
16 days
Performing Laboratory Location The location of the laboratory that performs the test
Rochester
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