Allele Registry

Canonical Allele Identifier: PA110014

Gene: SLC2A1 HGNC NCBI

ClinVar RCV:

RCV000189355

RCV000546488

RCV000763337

RCV002288795

RCV004525897

RCV004539756

ClinVar Variation:

207193

HGVS (amino-acid)	Matching Registered Transcripts
NP_006507.2:p.Arg223Trp	CA318433 NM_006516.4:c.667C>T