Canonical Allele Identifier: PA171825
Gene: D2HGDH HGNC NCBI

Linked Data

ClinVar Variation Id: 158410
ClinVar RCV Id: RCV000145791 RCV000444247 RCV000987080 RCV003917442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_689996.4:p.Ala426Thr
CA171824
NM_152783.5:c.1276G>A