Canonical Allele Identifier: PA2825576879
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 953372

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gly1530Asp
CA394305086
NM_001114382.3:c.4589G>A