Allele Registry

Canonical Allele Identifier: PA207100

Gene: D2HGDH HGNC NCBI

ClinVar RCV:

RCV000193545

RCV000514436

RCV001084317

ClinVar Variation:

210810

HGVS (amino-acid)	Matching Registered Transcripts
NP_689996.4:p.Gly355Ser	CA207099 NM_152783.5:c.1063G>A