Canonical Allele Identifier: PA2828621949
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001362537.1:p.Ala282Val
CA114391
NM_001375608.1:c.845C>T