Canonical Allele Identifier: PA2828042441
Gene: SLC35E3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2389608
ClinVar RCV Id: RCV004231747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341926.1:p.Tyr122Cys
CA6678298
NM_001354997.3:c.365A>G