Canonical Allele Identifier: PA915986886
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466161

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Cys306Tyr
CA039723
NM_001162426.2:c.917G>A