Allele Registry

Canonical Allele Identifier: PA2828418099

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535899

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357334.1:p.Gly671Asp	CA035599 NM_001370405.1:c.2012G>A