Canonical Allele Identifier: PA915987180
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 466150

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.Arg22Gln
CA038390
NM_001162427.2:c.65G>A