Allele Registry

Canonical Allele Identifier: PA2829972020

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 480835

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Tyr274Cys	CA394313259 NM_021055.3:c.821A>G