Canonical Allele Identifier: PA2826742009
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1494698
ClinVar RCV Id: RCV002015073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001274178.1:p.Asn309Ser
CA2222205
NM_001287249.2:c.926A>G