Allele Registry

Canonical Allele Identifier: PA2825575139

Gene: TSC2 HGNC NCBI

ClinVar Allele:

401519

ClinVar RCV:

RCV000475335

RCV000761103

RCV002436402

ClinVar Variation:

406089

HGVS (amino-acid)	Matching Registered Transcripts
NP_001107854.1:p.Asp1013Gly	CA16615087 NM_001114382.3:c.3038A>G