Allele Registry

Canonical Allele Identifier: PA114768

Gene: AGL HGNC NCBI

ClinVar RCV:

RCV000001166

ClinVar Variation:

1107

HGVS (amino-acid)	Matching Registered Transcripts
NP_000633.2:p.Arg1147Gly	CA114767 NM_000642.3:c.3439A>G