Allele Registry

Canonical Allele Identifier: PA2827013154

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406039

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Pro472Leu	CA16615063 NM_001318831.2:c.1415C>T