Canonical Allele Identifier: PA2826741969
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1858
ClinVar RCV Id: RCV000001932
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274178.1:p.Asp241Tyr
CA115239
NM_001287249.2:c.721G>T