Allele Registry

Canonical Allele Identifier: PA2828411009

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000226213

RCV000568157

ClinVar Variation:

237961

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Glu405Gln	CA028805 NM_001370404.1:c.1213G>C