Allele Registry

Canonical Allele Identifier: PA2829978799

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406107

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser1089Leu	CA046484 NM_021055.3:c.3266C>T