Allele Registry

Canonical Allele Identifier: PA2827004856

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644175

ClinVar Variation:

535941

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305756.1:p.Tyr1468His	CA394307381 NM_001318827.2:c.4402T>C