Allele Registry

Canonical Allele Identifier: PA2829980105

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000122230

RCV000644130

RCV001021539

RCV003628312

RCV003997366

ClinVar Variation:

135384

2837265

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu1278Asp	CA019763 NM_021055.3:c.3834G>C CA394297480 NM_021055.3:c.3834G>T