Canonical Allele Identifier: PA2826661694
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 507814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Arg134Cys
CA10406067
NM_001282648.2:c.400C>T