Canonical Allele Identifier: PA645475902
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_064425.2:p.Arg294His
CA2857052
NM_020041.3:c.881G>A