Allele Registry

Canonical Allele Identifier: PA104655

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000004860

RCV001851656

ClinVar Variation:

4597

HGVS (amino-acid)	Matching Registered Transcripts
NP_064425.2:p.Arg198Cys	CA116941 NM_020041.3:c.592C>T