Allele Registry

Canonical Allele Identifier: PA102936

Gene: GNE HGNC NCBI

ClinVar RCV:

RCV000594398

RCV000597478

RCV001214147

ClinVar Variation:

290196

HGVS (amino-acid)	Matching Registered Transcripts
NP_005467.1:p.Arg162Cys	CA5056722 NM_005476.7:c.484C>T