Canonical Allele Identifier: PA2829588756
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2416741
ClinVar RCV Id: RCV003108992

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Gln493His
CA5056476
NM_005476.7:c.1479A>C
CA373426695
NM_005476.7:c.1479A>T