Allele Registry

Canonical Allele Identifier: PA116944

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000004861

ClinVar Variation:

4598

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001290.1:p.Pro383Arg	CA116943 NM_001001290.2:c.1148C>G