Allele Registry

Canonical Allele Identifier: PA2828416796

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000394048

RCV000570041

RCV001089419

ClinVar Variation:

283532

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Phe298Ser	CA056651 NM_001370405.1:c.893T>C