Allele Registry

Canonical Allele Identifier: PA2828414419

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Gly1399Val	CA394301384 NM_001370404.1:c.4196G>T