Allele Registry

Canonical Allele Identifier: PA2827018844

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV004520826

ClinVar Variation:

3232143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305761.1:p.Ser1099Trp	CA394286828 NM_001318832.2:c.3296C>G