Allele Registry

Canonical Allele Identifier: PA2828413368

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV004520826

ClinVar Variation:

3232143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Ser1088Trp	CA394286828 NM_001370404.1:c.3263C>G