Allele Registry

Canonical Allele Identifier: PA2828420211

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000531608

ClinVar Variation:

468059

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Ser1297Phe	CA050173 NM_001370405.1:c.3890C>T