Allele Registry

Canonical Allele Identifier: PA2826157822

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000593521

RCV001854024

RCV003459467

ClinVar Variation:

498627

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177312.1:p.Ser594Phe	CA373424635 NM_001190383.3:c.1781C>T