Canonical Allele Identifier: PA111706
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Gly334Ser
CA114406
NM_000312.4:c.1000G>A