Canonical Allele Identifier: PA2827005090
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 197025

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.His1537Pro
CA021276
NM_001318827.2:c.4610A>C