Allele Registry

Canonical Allele Identifier: PA2825369782

Gene: GLUL HGNC NCBI

ClinVar RCV:

RCV000022586

ClinVar Variation:

29734

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028228.1:p.Arg324Ser	CA128603 NM_001033056.4:c.970C>A