Allele Registry

Canonical Allele Identifier: PA916013641

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000210405

ClinVar Variation:

224808

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269580.1:p.Tyr295Cys	CA357924 NM_001282651.2:c.884A>G