Allele Registry

Canonical Allele Identifier: PA2827015799

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000644175

ClinVar Variation:

535941

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Tyr1327His	CA394307381 NM_001318831.2:c.3979T>C