Allele Registry

Canonical Allele Identifier: PA2827012882

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535880

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Pro405Leu	CA394272977 NM_001318831.2:c.1214C>T