Allele Registry

Canonical Allele Identifier: PA2829588505

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV001782212

ClinVar Variation:

1324492

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Asp378His	CA373428995 NM_005476.7:c.1132G>C