Canonical Allele Identifier: PA2827683271
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 1448519
ClinVar RCV Id: RCV002012174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001339753.1:p.Pro264Ser
CA2222210
NM_001352824.2:c.790C>T