Allele Registry

Canonical Allele Identifier: PA2829980743

Gene: TSC2 HGNC NCBI

ClinVar Allele:

466067

ClinVar RCV:

RCV000540815

RCV001672838

RCV002330897

RCV003999309

ClinVar Variation:

468071

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Arg1366Gly	CA276753368 NM_021055.3:c.4096C>G