Canonical Allele Identifier: PA2825574517
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val789Ile
CA038777
NM_001114382.3:c.2365G>A