Canonical Allele Identifier: PA102875
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Ala460Val
CA253707
NM_005476.7:c.1379C>T