Allele Registry

Canonical Allele Identifier: PA116945

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000004861

ClinVar Variation:

4598

HGVS (amino-acid)	Matching Registered Transcripts
NP_064425.2:p.Pro412Arg	CA116943 NM_020041.3:c.1235C>G