Canonical Allele Identifier: PA2825954979
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Lys117Thr
CA200901566
NM_001162427.2:c.350A>C