Canonical Allele Identifier: PA2825957100
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Arg717His
CA16612757
NM_001162427.2:c.2150G>A