Allele Registry

Canonical Allele Identifier: PA916013616

Gene: SLC35A2 HGNC NCBI

ClinVar Allele:

446897

ClinVar RCV:

RCV000560194

ClinVar Variation:

453301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269579.1:p.Cys95Phe	CA412897640 NM_001282650.2:c.284G>T