Allele Registry

Canonical Allele Identifier: PA916023691

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000444052

RCV000546851

RCV000767144

RCV002411311

ClinVar Variation:

379559

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Gly641Asp	CA16606929 NM_001318832.2:c.1922G>A