Allele Registry

Canonical Allele Identifier: PA2828411334

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000543764

RCV002256373

RCV003999254

ClinVar Variation:

467878

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Arg505Gly	CA394326162 NM_001370404.1:c.1513C>G