Canonical Allele Identifier: PA2826661701
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1092796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Arg139Cys
CA412894179
NM_001282648.2:c.415C>T