Allele Registry

Canonical Allele Identifier: PA2825575532

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV004520826

ClinVar Variation:

3232143

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Ser1132Trp	CA394286828 NM_001114382.3:c.3395C>G