Allele Registry

Canonical Allele Identifier: PA1139743836

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000276478

RCV003230473

ClinVar Variation:

288301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361727.1:p.Ile47Thr	CA5056733 NM_001374798.1:c.140T>C