Canonical Allele Identifier: PA102926
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6035

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Ala631Val
CA253717
NM_005476.7:c.1892C>T