Allele Registry

Canonical Allele Identifier: PA2827009827

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055306

RCV003512006

ClinVar Variation:

65095

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Leu1433Pro	CA020803 NM_001318829.2:c.4298T>C