Canonical Allele Identifier: PA2825574106
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala675Leu
CA658658369
NM_001114382.3:c.2023_2024delinsTT