Allele Registry

Canonical Allele Identifier: PA114398

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV000000697

RCV000689442

RCV003985071

ClinVar Variation:

662

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Ala309Thr	CA114396 NM_000312.4:c.925G>A