Canonical Allele Identifier: PA2825955039
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466148

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Ala135Thr
CA375372741
NM_001162427.2:c.403G>A