Canonical Allele Identifier: PA2826158248
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 6033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Val462Leu
CA274932
NM_001190384.3:c.1384G>C
CA373425687
NM_001190384.3:c.1384G>T