Allele Registry

Canonical Allele Identifier: PA2827006555

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000462431

RCV002393093

ClinVar Variation:

406037

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Ile297Val	CA16615037 NM_001318829.2:c.889A>G