Allele Registry

Canonical Allele Identifier: PA2829589218

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000593521

RCV001854024

RCV003459467

ClinVar Variation:

498627

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Ser668Phe	CA373424635 NM_005476.7:c.2003C>T