Canonical Allele Identifier: PA095242
Gene: GCDH HGNC NCBI

Linked Data

ClinVar Variation Id: 2082
ClinVar RCV Id: RCV000002163 RCV000224804
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000150.1:p.Ala421Val
CA252095
NM_000159.4:c.1262C>T