Allele Registry

Canonical Allele Identifier: PA2828092183

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 207669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.His763Tyr	CA038145 NM_001363528.2:c.2287C>T