Canonical Allele Identifier: PA2825954725
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155898.1:p.Lys168Thr
CA200901566
NM_001162426.2:c.503A>C