Canonical Allele Identifier: PA915987414
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001155899.1:p.His956Tyr
CA035635
NM_001162427.2:c.2866C>T