Allele Registry

Canonical Allele Identifier: PA2826157567

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000169197

RCV000726859

RCV001041020

ClinVar Variation:

188847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177312.1:p.Arg277Cys	CA274033 NM_001190383.3:c.829C>T