Allele Registry

Canonical Allele Identifier: PA2828413229

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000221766

RCV001341323

RCV002251447

ClinVar Variation:

233995

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357333.1:p.Ser1050Trp	CA045126 NM_001370404.1:c.3149C>G