Allele Registry

Canonical Allele Identifier: PA357925

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000210405

ClinVar Variation:

224808

HGVS (amino-acid)	Matching Registered Transcripts
NP_005651.1:p.Tyr267Cys	CA357924 NM_005660.3:c.800A>G