Allele Registry

Canonical Allele Identifier: PA102960

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000178150

RCV000700059

RCV000984181

ClinVar Variation:

197184

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Arg246Trp	CA275247 NM_005476.7:c.736C>T