Allele Registry

Canonical Allele Identifier: PA126192

Gene: GLUL HGNC NCBI

ClinVar RCV:

RCV000017463

ClinVar Variation:

16083

HGVS (amino-acid)	Matching Registered Transcripts
NP_002056.2:p.Arg324Cys	CA126191 NM_002065.7:c.970C>T