Allele Registry

Canonical Allele Identifier: PA2827015318

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Gly1199Val	CA394301384 NM_001318831.2:c.3596G>T