Allele Registry

Canonical Allele Identifier: PA3057500361

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV005112357

ClinVar Variation:

3637238

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Glu1399Gly	CA394301357 NM_021055.3:c.4196A>G