Allele Registry

Canonical Allele Identifier: PA264566

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000055315

RCV000055380

RCV000189909

RCV000562671

RCV000644061

ClinVar Variation:

65104

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Pro878Ser	CA017740 NM_000548.5:c.2632C>T