Allele Registry

Canonical Allele Identifier: PA2827014972

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000531608

ClinVar Variation:

468059

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Ser1096Phe	CA050173 NM_001318831.2:c.3287C>T