Allele Registry

Canonical Allele Identifier: PA111642

Gene: PROC HGNC NCBI

ClinVar Allele:

171070

ClinVar RCV:

RCV000148740

RCV000851669

ClinVar Variation:

161334

HGVS (amino-acid)	Matching Registered Transcripts
NP_000303.1:p.Asp401Asn	CA211710 NM_000312.4:c.1201G>A