Canonical Allele Identifier: PA916023210
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Lys80Glu
CA036103
NM_001318832.2:c.238A>G