Canonical Allele Identifier: PA2826158172
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2941761
ClinVar RCV Id: RCV003802783

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Thr379Ile
CA373426760
NM_001190384.3:c.1136C>T