Allele Registry

Canonical Allele Identifier: PA111632

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV000168170

RCV000490205

RCV002498834

ClinVar Variation:

188230

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Arg57Trp	CA334388 NM_000312.4:c.169C>T