Canonical Allele Identifier: PA2829580912
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167722
ClinVar RCV Id: RCV001517306
ClinVar Variation Id: 2579713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Gly357Arg
CA10406062
NM_005660.3:c.1069G>C
CA10406063
NM_005660.3:c.1069G>A