Canonical Allele Identifier: PA915970390
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 627242
ClinVar RCV Id: RCV000852033

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001121699.1:p.Leu517Pro
CA5056478
NM_001128227.3:c.1550T>C