Allele Registry

Canonical Allele Identifier: PA2827003455

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 373567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Ser1072Arg	CA046905 NM_001318827.2:c.3214A>C CA394288809 NM_001318827.2:c.3216T>A CA394288819 NM_001318827.2:c.3216T>G