Canonical Allele Identifier: PA2828550500
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 501311
ClinVar RCV Id: RCV000592843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.His458Pro
CA373426459
NM_001374797.1:c.1373A>C