Allele Registry

Canonical Allele Identifier: PA2826662063

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000210405

ClinVar Variation:

224808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269579.1:p.Tyr280Cys	CA357924 NM_001282650.2:c.839A>G