Allele Registry

Canonical Allele Identifier: PA2828413168

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000457622

RCV002446790

ClinVar Variation:

406055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Arg1034Gln	CA044900 NM_001370404.1:c.3101G>A