Allele Registry

Canonical Allele Identifier: PA2825574857

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000190005

RCV000644168

RCV002426918

ClinVar Variation:

207734

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Ile893Thr	CA319484 NM_001114382.3:c.2678T>C