Allele Registry

Canonical Allele Identifier: PA645407518

Gene: D2HGDH HGNC NCBI

ClinVar RCV:

RCV000344675

RCV000513354

RCV003957730

RCV004021807

ClinVar Variation:

335320

HGVS (amino-acid)	Matching Registered Transcripts
NP_689996.4:p.Val485Ile	CA2222239 NM_152783.5:c.1453G>A