Canonical Allele Identifier: PA916047990
Gene: PRSS56 HGNC NCBI

Linked Data

ClinVar Variation Id: 31079
ClinVar RCV Id: RCV000024075
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356777.1:p.Trp309Ser
CA129652
NM_001369848.1:c.926G>C