Allele Registry

Canonical Allele Identifier: PA2828418271

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000518165

ClinVar Variation:

448724

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Leu717Gln	CA394274849 NM_001370405.1:c.2150T>A