Canonical Allele Identifier: PA2826158582
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 281291
ClinVar RCV Id: RCV000344814 RCV001208464 RCV001833307
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Arg276Trp
CA5056603
NM_001190388.2:c.826C>T