Allele Registry

Canonical Allele Identifier: PA2827014936

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000460658

RCV000607342

RCV001021602

RCV004000727

ClinVar Variation:

406131

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Asp1087Glu	CA049880 NM_001318831.2:c.3261T>A CA394297754 NM_001318831.2:c.3261T>G