Canonical Allele Identifier: PA2825955107
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Met158Val
CA038277
NM_001162427.2:c.472A>G