Canonical Allele Identifier: PA915970237
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 827569
ClinVar RCV Id: RCV002445198
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Tyr28Asp
CA369607137
NM_002769.5:c.82T>G