Allele Registry

Canonical Allele Identifier: PA2826741960

Gene: D2HGDH HGNC NCBI

ClinVar RCV:

RCV000193545

RCV000514436

RCV001084317

ClinVar Variation:

210810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274178.1:p.Gly221Ser	CA207099 NM_001287249.2:c.661G>A