Canonical Allele Identifier: PA2825215300
Gene: SLC2A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 350213
ClinVar RCV Id: RCV000317105 RCV001509694
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001290.1:p.Arg265His
CA2857052
NM_001001290.2:c.794G>A