Allele Registry

Canonical Allele Identifier: PA2829977995

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 406089

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Asp970Gly	CA16615087 NM_021055.3:c.2909A>G