Canonical Allele Identifier: PA2827005510
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1642Cys
CA054522
NM_001318827.2:c.4924C>T