Canonical Allele Identifier: PA2825957707
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Leu914Ile
CA16612444
NM_001162427.2:c.2740T>A