Allele Registry

Canonical Allele Identifier: PA210118

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000201283

ClinVar Variation:

217421

HGVS (amino-acid)	Matching Registered Transcripts
NP_001001290.1:p.Thr96Met	CA210117 NM_001001290.2:c.287C>T