Allele Registry

Canonical Allele Identifier: PA916047996

Gene: PRSS56 HGNC NCBI

ClinVar RCV:

RCV000024074

RCV000454640

RCV001610296

ClinVar Variation:

31078

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356777.1:p.Pro600Ala	CA129651 NM_001369848.1:c.1798C>G