Allele Registry

Canonical Allele Identifier: PA2825575600

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 373567

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Ser1152Arg	CA046905 NM_001114382.3:c.3454A>C CA394288809 NM_001114382.3:c.3456T>A CA394288819 NM_001114382.3:c.3456T>G