Allele Registry

Canonical Allele Identifier: PA2825369784

Gene: GLUL HGNC NCBI

ClinVar RCV:

RCV000017463

ClinVar Variation:

16083

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028228.1:p.Arg324Cys	CA126191 NM_001033056.4:c.970C>T