Canonical Allele Identifier: PA2826157980
Gene: GNE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Arg153Leu
CA340505
NM_001190384.3:c.458G>T