Allele Registry

Canonical Allele Identifier: PA645469197

Gene: SLC2A10 HGNC NCBI

ClinVar Variation Id: 264101

HGVS (amino-acid)	Matching Registered Transcripts
NP_110404.1:p.Thr194Ile	CA9892002 NM_030777.4:c.581C>T