Allele Registry

Canonical Allele Identifier: PA2829977995

Gene: TSC2 HGNC NCBI

ClinVar RCV:

RCV000475335

RCV000761103

RCV002436402

ClinVar Variation:

406089

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