Allele Registry

Canonical Allele Identifier: PA264731

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055558

RCV001824119

ClinVar Variation:

65334

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.His597Tyr	CA015730 NM_000548.5:c.1789C>T