Allele Registry

Canonical Allele Identifier: PA645423569

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000400388

RCV000534256

RCV000657912

RCV003323497

ClinVar Variation:

290713

HGVS (amino-acid)	Matching Registered Transcripts
NP_001121699.1:p.Arg102Trp	CA10606885 NM_001128227.3:c.304A>T