Allele Registry

Canonical Allele Identifier: PA2825410777

Gene: SLC35A2 HGNC NCBI

ClinVar Allele:

438444

ClinVar RCV:

RCV000513019

RCV001511787

ClinVar Variation:

444804

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035963.1:p.Ala347Thr	CA10406070 NM_001042498.3:c.1039G>A