Allele Registry

Canonical Allele Identifier: PA102895

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000494055

RCV000675176

RCV001385137

ClinVar Variation:

286014

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Ala600Thr	CA10605332 NM_005476.7:c.1798G>A