Canonical Allele Identifier: PA2826158190
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 501311
ClinVar RCV Id: RCV000592843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.His399Pro
CA373426459
NM_001190384.3:c.1196A>C