Allele Registry

Canonical Allele Identifier: PA2828419798

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 1718047

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Ser1174Arg	CA394291960 NM_001370405.1:c.3520A>C CA394291979 NM_001370405.1:c.3522C>A CA394291987 NM_001370405.1:c.3522C>G