Canonical Allele Identifier: PA2825957731
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207617

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Lys925Glu
CA319252
NM_001162427.2:c.2773A>G