Canonical Allele Identifier: PA2828059399
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411227

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.Ser194Thr
CA039861
NM_001362177.1:c.580T>A