Allele Registry

Canonical Allele Identifier: PA2825575291

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 318325

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Leu1066Phe	CA10648022 NM_001114382.3:c.3196C>T