Allele Registry

Canonical Allele Identifier: PA2829983913

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_066399.2:p.Ser1731Thr	CA022390 NM_021055.3:c.5192G>C