Allele Registry

Canonical Allele Identifier: PA2826157608

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000344814

RCV001208464

RCV001833307

ClinVar Variation:

281291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177312.1:p.Arg335Trp	CA5056603 NM_001190383.3:c.1003C>T