Allele Registry

Canonical Allele Identifier: PA105190

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000122746

ClinVar Variation:

135676

HGVS (amino-acid)	Matching Registered Transcripts
NP_005651.1:p.Ser213Phe	CA163127 NM_005660.3:c.638C>T