Allele Registry

Canonical Allele Identifier: PA2825885692

Gene: SLC17A8 HGNC NCBI

ClinVar RCV:

RCV000003256

RCV000724921

ClinVar Variation:

3109

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138760.1:p.Ala211Val	CA252550 NM_001145288.2:c.632C>T