Allele Registry

Canonical Allele Identifier: PA2829976361

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 374680

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Arg786Cys	CA038725 NM_021055.3:c.2356C>T