Canonical Allele Identifier: PA2825362138
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2579713

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001027460.1:p.Arg160Pro
CA10406062
NM_001032289.3:c.479G>C