Canonical Allele Identifier: PA2825576876
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1529del
CA020824
NM_001114382.3:c.4586_4588del