Canonical Allele Identifier: PA1139675322
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Pro1265del
CA10579895
NM_001114382.3:c.3794_3796del