Canonical Allele Identifier: PA2826157851
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 194025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177312.1:p.Val622Leu
CA239806
NM_001190383.3:c.1864G>T
CA373424372
NM_001190383.3:c.1864G>C