Canonical Allele Identifier: PA2828061082
Gene: TSC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 411246

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001349106.1:p.His886Tyr
CA035635
NM_001362177.1:c.2656C>T