Allele Registry

Canonical Allele Identifier: PA2826662035

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000122746

ClinVar Variation:

135676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269579.1:p.Ser226Phe	CA163127 NM_001282650.2:c.677C>T