Allele Registry

Canonical Allele Identifier: PA2827010367

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644161

RCV002334132

ClinVar Variation:

535931

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.His1611Tyr	CA054330 NM_001318829.2:c.4831C>T