Allele Registry

Canonical Allele Identifier: PA111564

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV000000693

RCV000000694

RCV000851836

ClinVar Variation:

659

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Arg211Trp	CA114389 NM_000312.4:c.631C>T