Allele Registry

Canonical Allele Identifier: PA126194

Gene: GLUL HGNC NCBI

ClinVar RCV:

RCV000017464

ClinVar Variation:

16084

HGVS (amino-acid)	Matching Registered Transcripts
NP_002056.2:p.Arg341Cys	CA126193 NM_002065.7:c.1021C>T