Canonical Allele Identifier: PA2827005372
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406029

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1610Cys
CA054033
NM_001318827.2:c.4828C>T