Canonical Allele Identifier: PA2829588192
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1475667
ClinVar RCV Id: RCV001976418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005467.1:p.Asp196His
CA373418026
NM_005476.7:c.586G>C