Canonical Allele Identifier: PA2580263738
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1752175
ClinVar RCV Id: RCV002366448

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Asp21His
CA369607059
NM_002769.5:c.61G>C