Canonical Allele Identifier: PA2825575698
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1179Lys
CA019256
NM_001114382.3:c.3535G>A