Canonical Allele Identifier: PA2826157551
Gene: GNE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Arg263Leu
CA340505
NM_001190383.3:c.788G>T