Allele Registry

Canonical Allele Identifier: PA2826742033

Gene: D2HGDH HGNC NCBI

ClinVar RCV:

RCV000344675

RCV000513354

RCV003957730

RCV004021807

ClinVar Variation:

335320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274178.1:p.Val351Ile	CA2222239 NM_001287249.2:c.1051G>A