Allele Registry

Canonical Allele Identifier: PA916023014

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000189915

RCV000490959

RCV000546326

ClinVar Variation:

207676

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305760.1:p.Pro865Leu	CA319368 NM_001318831.2:c.2594C>T