Allele Registry

Canonical Allele Identifier: PA916047993

Gene: PRSS56 HGNC NCBI

ClinVar RCV:

RCV000171337

RCV002515237

ClinVar Variation:

191153

HGVS (amino-acid)	Matching Registered Transcripts
NP_001356777.1:p.Arg468Leu	CA236128 NM_001369848.1:c.1403G>T