Canonical Allele Identifier: PA2825576852
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 825059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ala1523Thr
CA394304918
NM_001114382.3:c.4567G>A