Allele Registry

Canonical Allele Identifier: PA2828414074

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000531608

ClinVar Variation:

468059

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Ser1296Phe	CA050173 NM_001370404.1:c.3887C>T