Canonical Allele Identifier: PA2825070164
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 971376
ClinVar RCV Id: RCV001247144 RCV001252002 RCV004034887
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala316Thr
CA9234551
NM_000159.4:c.946G>A