Canonical Allele Identifier: PA2825955057
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 49061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Leu140Arg
CA007790
NM_001162427.2:c.419T>G