Canonical Allele Identifier: PA2826661630
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1194058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269576.1:p.Ala170Glu
CA412894117
NM_001282647.2:c.509C>A