Allele Registry

Canonical Allele Identifier: PA2829983918

Gene: TSC2 HGNC NCBI

ClinVar Variation Id: 468157

HGVS (amino-acid)	Matching Registered Transcripts
NP_066399.2:p.Ser1731Gly	CA055089 NM_021055.3:c.5191A>G