Allele Registry

Canonical Allele Identifier: PA2829980709

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406008

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Asp1363Tyr	CA050670 NM_021055.3:c.4087G>T