Allele Registry

Canonical Allele Identifier: PA2826661835

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000210405

ClinVar Variation:

224808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269578.1:p.Tyr206Cys	CA357924 NM_001282649.2:c.617A>G