Canonical Allele Identifier: PA2826661891
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 754204
ClinVar RCV Id: RCV001523443

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Ala294Thr
CA10406065
NM_001282649.2:c.880G>A