Allele Registry

Canonical Allele Identifier: PA2825369792

Gene: GLUL HGNC NCBI

ClinVar RCV:

RCV000017464

ClinVar Variation:

16084

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028228.1:p.Arg341Cys	CA126193 NM_001033056.4:c.1021C>T