Canonical Allele Identifier: PA2825576084
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406131

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Asp1308Glu
CA049880
NM_001114382.3:c.3924T>A
CA394297754
NM_001114382.3:c.3924T>G