Allele Registry

Canonical Allele Identifier: PA2828421863

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001023976

RCV001204908

RCV001696827

ClinVar Variation:

449819

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Tyr1741Cys	CA055219 NM_001370405.1:c.5222A>G