Canonical Allele Identifier: PA095296
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2089
ClinVar RCV Id: RCV000002170 RCV000078256
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Arg227Pro
CA220441
NM_000159.4:c.680G>C