Allele Registry

Canonical Allele Identifier: PA2828411177

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000213492

RCV000473388

ClinVar Variation:

231820

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Glu456Gly	CA10579874 NM_001370404.1:c.1367A>G