Allele Registry

Canonical Allele Identifier: PA2827010027

Gene: TSC2 HGNC NCBI

ClinVar Allele:

58489

ClinVar RCV:

RCV000042587

RCV001383217

ClinVar Variation:

49327

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305758.1:p.His1505Tyr	CA021147 NM_001318829.2:c.4513C>T