Allele Registry

Canonical Allele Identifier: PA916023851

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 207669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.His774Tyr	CA038145 NM_001318832.2:c.2320C>T