Canonical Allele Identifier: PA111583
Gene: PROC HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Arg220Trp
CA114410
NM_000312.4:c.658C>T