Allele Registry

Canonical Allele Identifier: PA2828421040

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644175

ClinVar Variation:

535941

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Tyr1528His	CA394307381 NM_001370405.1:c.4582T>C