Allele Registry

Canonical Allele Identifier: PA104662

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000004859

RCV002512777

ClinVar Variation:

4596

HGVS (amino-acid)	Matching Registered Transcripts
NP_064425.2:p.Arg380Trp	CA116939 NM_020041.3:c.1138C>T