Allele Registry

Canonical Allele Identifier: PA2829980029

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000535896

RCV001021475

RCV001705074

RCV003996893

ClinVar Variation:

207749

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu1270Asp	CA049654 NM_021055.3:c.3810G>T CA394297301 NM_021055.3:c.3810G>C