Allele Registry

Canonical Allele Identifier: PA2827019830

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV001367751

ClinVar Variation:

1058594

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Gly1387Val	CA394301384 NM_001318832.2:c.4160G>T