Canonical Allele Identifier: PA2826158529
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6022

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Arg207Gln
CA340503
NM_001190388.2:c.620G>A