Canonical Allele Identifier: PA2826157879
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1716084
ClinVar RCV Id: RCV002295851
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Thr11Ala
CA373419911
NM_001190384.3:c.31A>G