Allele Registry

Canonical Allele Identifier: PA107697

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000042905

RCV000189989

RCV000491813

RCV000539587

RCV000768117

ClinVar Variation:

49643

HGVS (amino-acid)	Matching Registered Transcripts
NP_000539.2:p.Arg611Trp	CA015914 NM_000548.5:c.1831C>T CA645594269 NM_000548.5:c.1830_1831delinsTT