Allele Registry

Canonical Allele Identifier: PA2828090039

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV003628435

ClinVar Variation:

2844167

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350457.1:p.Glu141Gln	CA394307197 NM_001363528.2:c.421G>C