Allele Registry

Canonical Allele Identifier: PA2827008337

Gene: TSC2 HGNC NCBI

ClinVar Allele:

401519

ClinVar RCV:

RCV000475335

RCV000761103

RCV002436402

ClinVar Variation:

406089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.Asp921Gly	CA16615087 NM_001318829.2:c.2762A>G