Allele Registry

Canonical Allele Identifier: PA2827007814

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 207669

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.His714Tyr	CA038145 NM_001318829.2:c.2140C>T