Canonical Allele Identifier: PA103056
Gene: GNE HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Cys303Val
CA253712
NM_005476.7:c.907_908delinsGT