Canonical Allele Identifier: PA2826158459
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2052862
ClinVar RCV Id: RCV002937767

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Cys124Ser
CA373418196
NM_001190388.2:c.371G>C
CA373418200
NM_001190388.2:c.370T>A