Allele Registry

Canonical Allele Identifier: PA111669

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV000000699

RCV003398403

ClinVar Variation:

664

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Glu62Ala	CA114402 NM_000312.4:c.185A>C