Canonical Allele Identifier: PA171817
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 158406
ClinVar RCV Id: RCV000145787 RCV000370487 RCV000677011
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689996.4:p.Ala361Val
CA171816
NM_152783.5:c.1082C>T