Canonical Allele Identifier: PA2825918666
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411249

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Arg767His
CA16612757
NM_001162426.2:c.2300G>A