Canonical Allele Identifier: PA2827018473
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1717908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu967Met
CA394283761
NM_001318832.2:c.2899T>A