Allele Registry

Canonical Allele Identifier: PA2829981809

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 49479

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Tyr1506Cys	CA020809 NM_021055.3:c.4517A>G