Allele Registry

Canonical Allele Identifier: PA2828091062

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000213492

RCV000473388

ClinVar Variation:

231820

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Glu456Gly	CA10579874 NM_001363528.2:c.1367A>G