Allele Registry

Canonical Allele Identifier: PA2829970283

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 207655

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Thr36Ala	CA028094 NM_021055.3:c.106A>G