Allele Registry

Canonical Allele Identifier: PA186011

Gene: PRSS56 HGNC NCBI

ClinVar RCV:

RCV000162043

ClinVar Variation:

183175

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182058.1:p.Gly519Arg	CA186010 NM_001195129.2:c.1555G>A CA2167806 NM_001195129.2:c.1555G>C