Canonical Allele Identifier: PA107068
Gene: PRSS1 HGNC NCBI

Linked Data

ClinVar Variation Id: 29923
ClinVar RCV Id: RCV000022814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002760.1:p.Arg116Cys
CA342722
NM_002769.5:c.346C>T