Allele Registry

Canonical Allele Identifier: PA2827006862

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000470761

RCV001011130

RCV001591076

RCV004000707

ClinVar Variation:

406041

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Arg405Ser	CA029692 NM_001318829.2:c.1215G>C CA394323549 NM_001318829.2:c.1215G>T