Canonical Allele Identifier: PA102988
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6022
ClinVar RCV Id: RCV000006393 RCV001241785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Arg266Gln
CA340503
NM_005476.7:c.797G>A