Canonical Allele Identifier: PA2825574177
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 226045

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val692Ile
CA036245
NM_001114382.3:c.2074G>A