Canonical Allele Identifier: PA211717
Gene: PROC HGNC NCBI

Linked Data

ClinVar Variation Id: 161336

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000303.1:p.Gly412Ser
CA211715
NM_000312.4:c.1234G>A