Canonical Allele Identifier: PA916019540
Gene: PRSS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 8070
ClinVar RCV Id: RCV000008536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001290343.1:p.Gly205Arg
CA119273
NM_001303414.2:c.613G>A
CA458273422
NM_001303414.2:c.613G>C