Canonical Allele Identifier: PA2825215315
Gene: SLC2A9 HGNC NCBI

Linked Data

ClinVar Variation Id: 2276283
ClinVar RCV Id: RCV002827008
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001001290.1:p.Val291Leu
CA356400822
NM_001001290.2:c.871G>T
CA356400823
NM_001001290.2:c.871G>C