Allele Registry

Canonical Allele Identifier: PA2826157647

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000484722

RCV000596066

RCV000707707

RCV001165685

RCV004021128

ClinVar Variation:

283278

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177312.1:p.Asp378Tyr	CA5056560 NM_001190383.3:c.1132G>T