Allele Registry

Canonical Allele Identifier: PA2825437077

Gene: TSC2 HGNC NCBI

ClinVar Allele:

401519

ClinVar RCV:

RCV000475335

RCV000761103

RCV002436402

ClinVar Variation:

406089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001070651.1:p.Asp969Gly	CA16615087 NM_001077183.3:c.2906A>G