Allele Registry

Canonical Allele Identifier: PA2828418894

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000231440

RCV001016356

RCV003884383

ClinVar Variation:

207783

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Arg901Cys	CA319592 NM_001370405.1:c.2701C>T