Allele Registry

Canonical Allele Identifier: PA2827020072

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535877

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ser1451Tyr	CA051496 NM_001318832.2:c.4352C>A