Allele Registry

Canonical Allele Identifier: PA116942

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000004860

RCV001851656

ClinVar Variation:

4597

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001290.1:p.Arg169Cys	CA116941 NM_001001290.2:c.505C>T