Canonical Allele Identifier: PA2827012296
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 383175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.His235Tyr
CA029254
NM_001318831.2:c.703C>T