Allele Registry

Canonical Allele Identifier: PA2829975108

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 535899

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Gly671Asp	CA035599 NM_021055.3:c.2012G>A