Allele Registry

Canonical Allele Identifier: PA2825437229

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000467462

ClinVar Variation:

406049

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Thr1024Pro	CA16615089 NM_001077183.3:c.3070A>C