Allele Registry

Canonical Allele Identifier: PA2827009467

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Gly1328Val	CA394301384 NM_001318829.2:c.3983G>T