Allele Registry

Canonical Allele Identifier: PA2826157432

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000276478

RCV003230473

ClinVar Variation:

288301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177312.1:p.Ile106Thr	CA5056733 NM_001190383.3:c.317T>C