Allele Registry

Canonical Allele Identifier: PA2828413440

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 373567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Ser1108Arg	CA046905 NM_001370404.1:c.3322A>C CA394288809 NM_001370404.1:c.3324T>A CA394288819 NM_001370404.1:c.3324T>G