Canonical Allele Identifier: PA2826158712
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2062352
ClinVar RCV Id: RCV002923555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177317.2:p.Arg422Trp
CA5056480
NM_001190388.2:c.1264C>T