Canonical Allele Identifier: PA103216
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6028

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Val696Met
CA253688
NM_005476.7:c.2086G>A