Allele Registry

Canonical Allele Identifier: PA111592

Gene: PROC HGNC NCBI

ClinVar RCV:

RCV000000706

RCV000852227

ClinVar Variation:

671

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Arg272Cys	CA114414 NM_000312.4:c.814C>T