Allele Registry

Canonical Allele Identifier: PA171840

Gene: D2HGDH HGNC NCBI

ClinVar Variation Id: 158420

HGVS (amino-acid)	Matching Registered Transcripts
NP_689996.4:p.Arg15Gly	CA171839 NM_152783.5:c.43C>G