Canonical Allele Identifier: PA2826157721
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1402071
ClinVar RCV Id: RCV001913339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Ala457Thr
CA373427278
NM_001190383.3:c.1369G>A