Allele Registry

Canonical Allele Identifier: PA2826157408

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000400388

RCV000534256

RCV000657912

RCV003323497

ClinVar Variation:

290713

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177312.1:p.Arg71Trp	CA10606885 NM_001190383.3:c.211A>T