Allele Registry

Canonical Allele Identifier: PA916013633

Gene: SLC35A2 HGNC NCBI

ClinVar RCV:

RCV000122746

ClinVar Variation:

135676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269580.1:p.Ser241Phe	CA163127 NM_001282651.2:c.722C>T