Canonical Allele Identifier: PA2826157930
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1367872
ClinVar RCV Id: RCV001932589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Tyr97Cys
CA373418564
NM_001190384.3:c.290A>G