Allele Registry

Canonical Allele Identifier: PA2827020314

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644175

ClinVar Variation:

535941

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Tyr1515His	CA394307381 NM_001318832.2:c.4543T>C