Canonical Allele Identifier: PA2829588731
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2941698
ClinVar RCV Id: RCV003802720
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.His487Arg
CA373426773
NM_005476.7:c.1460A>G