Allele Registry

Canonical Allele Identifier: PA2829976462

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 467940

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Arg799Cys	CA394277095 NM_021055.3:c.2395C>T