Allele Registry

Canonical Allele Identifier: PA2826661807

Gene: SLC35A2 HGNC NCBI

ClinVar Allele:

139388

ClinVar RCV:

RCV000122746

ClinVar Variation:

135676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269578.1:p.Ser152Phe	CA163127 NM_001282649.2:c.455C>T