Canonical Allele Identifier: PA2580573316
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_999875.2:p.Ala66Thr
CA9022259
NM_214710.5:c.196G>A