Canonical Allele Identifier: PA2828551443
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_001361727.1:p.Thr430Ile
CA373426760
NM_001374798.1:c.1289C>T