Allele Registry

Canonical Allele Identifier: PA102996

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000006392

RCV001267416

ClinVar Variation:

6021

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Arg266Trp	CA340501 NM_005476.7:c.796C>T