Canonical Allele Identifier: PA2826661895
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167722
ClinVar RCV Id: RCV001517306
ClinVar Variation Id: 2579713
ClinVar RCV Id: RCV003328510 RCV003741345
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Gly296Arg
CA10406062
NM_001282649.2:c.886G>C
CA10406063
NM_001282649.2:c.886G>A