Allele Registry

Canonical Allele Identifier: PA2827683218

Gene: D2HGDH HGNC NCBI

ClinVar RCV:

RCV000193545

RCV000514436

RCV001084317

ClinVar Variation:

210810

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339753.1:p.Gly168Ser	CA207099 NM_001352824.2:c.502G>A