Canonical Allele Identifier: PA2826930223
Gene: PRSS57 HGNC NCBI

Linked Data

ClinVar Variation Id: 2390266
ClinVar RCV Id: RCV004229553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295138.2:p.Ala65Thr
CA9022259
NM_001308209.2:c.193G>A