Allele Registry

Canonical Allele Identifier: PA2825438386

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000530101

RCV000554219

RCV001022193

RCV001532308

RCV002330899

RCV003318590

ClinVar Variation:

468075

468076

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Gly1358Arg	CA050746 NM_001077183.3:c.4072G>A CA394300730 NM_001077183.3:c.4072G>C