Allele Registry

Canonical Allele Identifier: PA2828094244

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Gly1377Val	CA394301384 NM_001363528.2:c.4130G>T