Canonical Allele Identifier: PA2825574699
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406086

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu845Gly
CA039405
NM_001114382.3:c.2534A>G