Canonical Allele Identifier: PA2827005029
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65301

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Thr1520Ile
CA021153
NM_001318827.2:c.4559C>T