Allele Registry

Canonical Allele Identifier: PA2825438687

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535877

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Ser1440Tyr	CA051496 NM_001077183.3:c.4319C>A