Canonical Allele Identifier: PA2829588790
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 501311
ClinVar RCV Id: RCV000592843

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.His509Pro
CA373426459
NM_005476.7:c.1526A>C