Allele Registry

Canonical Allele Identifier: PA110549

Gene: PRSS56 HGNC NCBI

ClinVar RCV:

RCV000024074

RCV000454640

RCV001610296

ClinVar Variation:

31078

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182058.1:p.Pro599Ala	CA129651 NM_001195129.2:c.1795C>G