Canonical Allele Identifier: PA2828417237
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65257

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ser433Cys
CA014387
NM_001370405.1:c.1298C>G