Canonical Allele Identifier: PA357925
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224808
ClinVar RCV Id: RCV000210405
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Tyr267Cys
CA357924
NM_005660.3:c.800A>G