Canonical Allele Identifier: PA2826661620
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2038309
ClinVar RCV Id: RCV002890657

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269576.1:p.Arg160Trp
CA10406064
NM_001282647.2:c.478C>T