Allele Registry

Canonical Allele Identifier: PA916023639

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055558

RCV001824119

ClinVar Variation:

65334

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.His608Tyr	CA015730 NM_001318832.2:c.1822C>T