Canonical Allele Identifier: PA2828620997
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 660
ClinVar RCV Id: RCV000000695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362533.1:p.Ala322Val
CA114391
NM_001375604.1:c.965C>T