Canonical Allele Identifier: PA2827683267
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1494698
ClinVar RCV Id: RCV002015073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339753.1:p.Asn256Ser
CA2222205
NM_001352824.2:c.767A>G