Canonical Allele Identifier: PA2829611474
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2663778
ClinVar RCV Id: RCV003885329
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Leu307_Val310dup
CA2740092153
NM_005660.3:c.918_929dup