Canonical Allele Identifier: PA107059
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 38363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Ala16Val
CA342997
NM_002769.5:c.47C>T