Allele Registry

Canonical Allele Identifier: PA236129

Gene: PRSS56 HGNC NCBI

ClinVar RCV:

RCV000171337

RCV002515237

ClinVar Variation:

191153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001182058.1:p.Arg467Leu	CA236128 NM_001195129.2:c.1400G>T