Allele Registry

Canonical Allele Identifier: PA2827007677

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000518165

ClinVar Variation:

448724

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Leu668Gln	CA394274849 NM_001318829.2:c.2003T>A