Allele Registry

Canonical Allele Identifier: PA2826661886

Gene: SLC35A2 HGNC NCBI

ClinVar Allele:

438444

ClinVar RCV:

RCV000513019

RCV001511787

ClinVar Variation:

444804

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269578.1:p.Ala286Thr	CA10406070 NM_001282649.2:c.856G>A