Allele Registry

Canonical Allele Identifier: PA2828089875

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 467968

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Arg93Trp	CA041936 NM_001363528.2:c.277C>T