Allele Registry

Canonical Allele Identifier: PA116940

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000004859

RCV002512777

ClinVar Variation:

4596

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001290.1:p.Arg351Trp	CA116939 NM_001001290.2:c.1051C>T