Canonical Allele Identifier: PA2828549949
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 1367872
ClinVar RCV Id: RCV001932589

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361726.1:p.Tyr156Cys
CA373418564
NM_001374797.1:c.467A>G