Allele Registry

Canonical Allele Identifier: PA2827010796

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644175

ClinVar Variation:

535941

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Tyr1456His	CA394307381 NM_001318829.2:c.4366T>C