Canonical Allele Identifier: PA2828091933
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350457.1:p.Arg691Cys
CA016553
NM_001363528.2:c.2071C>T