Canonical Allele Identifier: PA916023884
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Val800Ile
CA038777
NM_001318832.2:c.2398G>A