Allele Registry

Canonical Allele Identifier: PA2829977704

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 49233

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Phe933Cys	CA018204 NM_021055.3:c.2798T>G