Canonical Allele Identifier: PA2826157447
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2663941
ClinVar RCV Id: RCV003444403
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Leu131Pro
CA373419033
NM_001190383.3:c.392T>C