Canonical Allele Identifier: PA2826157956
Gene: GNE HGNC NCBI

Linked Data

ClinVar Variation Id: 2136776
ClinVar RCV Id: RCV003062213

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001177313.1:p.Tyr127His
CA373418165
NM_001190384.3:c.379T>C