Allele Registry

Canonical Allele Identifier: PA114427

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV000000712

RCV001266003

RCV001781151

ClinVar Variation:

677

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Val339Met	CA114425 NM_000312.4:c.1015G>A