Canonical Allele Identifier: PA2826157949
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 41233
ClinVar RCV Id: RCV000343796 RCV000726858 RCV001060883
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Asp117Val
CA344238
NM_001190384.3:c.350A>T