Canonical Allele Identifier: PA2826661877
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50364
ClinVar RCV Id: RCV000043515 RCV000498343
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Val270Ile
CA143742
NM_001282649.2:c.808G>A