Canonical Allele Identifier: PA2826661886
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 444804
ClinVar RCV Id: RCV000513019 RCV001511787
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Ala286Thr
CA10406070
NM_001282649.2:c.856G>A