Allele Registry

Canonical Allele Identifier: PA2826742005

Gene: D2HGDH HGNC NCBI

ClinVar Allele:

1925529

ClinVar RCV:

RCV002664290

ClinVar Variation:

2203300

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274178.1:p.Gly302Val	CA351412860 NM_001287249.2:c.905G>T