Canonical Allele Identifier: PA2826158718
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2941761
ClinVar RCV Id: RCV003802783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Thr430Ile
CA373426760
NM_001190388.2:c.1289C>T