Allele Registry

Canonical Allele Identifier: PA2829974581

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406129

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Arg628Cys	CA034358 NM_021055.3:c.1882C>T