Canonical Allele Identifier: PA2826742028
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 653495
ClinVar RCV Id: RCV000809282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274178.1:p.Ala340Val
CA2222230
NM_001287249.2:c.1019C>T