Allele Registry

Canonical Allele Identifier: PA102926

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000006406

RCV000254883

RCV000763617

RCV004525844

ClinVar Variation:

6035

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Ala631Val	CA253717 NM_005476.7:c.1892C>T