Canonical Allele Identifier: PA101599
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1852
ClinVar RCV Id: RCV000001926
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689996.4:p.Val444Ala
CA115236
NM_152783.5:c.1331T>C