Allele Registry

Canonical Allele Identifier: PA2829971150

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV003628435

ClinVar Variation:

2844167

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu141Gln	CA394307197 NM_021055.3:c.421G>C