Allele Registry

Canonical Allele Identifier: PA2827021096

Gene: TSC2 HGNC NCBI

ClinVar Allele:

50184

ClinVar RCV:

RCV000034662

RCV000054870

RCV000118714

RCV000163420

RCV001084407

RCV002482951

ClinVar Variation:

41745

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ser1718Thr	CA022390 NM_001318832.2:c.5153G>C