Canonical Allele Identifier: PA2826158731
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 499667
ClinVar RCV Id: RCV000591966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Leu445Phe
CA5056473
NM_001190388.2:c.1333C>T