Canonical Allele Identifier: PA2825574172
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 184386

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Arg691Cys
CA016553
NM_001114382.3:c.2071C>T