Canonical Allele Identifier: PA2826930218
Gene: PRSS57 HGNC NCBI

Linked Data

ClinVar Variation Id: 207874
ClinVar RCV Id: RCV000190161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295138.2:p.Gly30Val
CA204125
NM_001308209.2:c.89G>T