Canonical Allele Identifier: PA2573304697
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1494698
ClinVar RCV Id: RCV002015073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689996.4:p.Asn443Ser
CA2222205
NM_152783.5:c.1328A>G