Allele Registry

Canonical Allele Identifier: PA2829972988

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 467858

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Tyr429Cys	CA029149 NM_021055.3:c.1286A>G