Canonical Allele Identifier: PA2826661618
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1167722
ClinVar RCV Id: RCV001517306
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269576.1:p.Arg160Gln
CA10406063
NM_001282647.2:c.479G>A