Canonical Allele Identifier: PA2825576745
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile1495Val
CA051585
NM_001114382.3:c.4483A>G