Canonical Allele Identifier: PA2826661692
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 589375
ClinVar RCV Id: RCV000862426 RCV002318788
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269577.1:p.Cys132Arg
CA10406068
NM_001282648.2:c.394T>C