Canonical Allele Identifier: PA2825435850
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65334

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.His597Tyr
CA015730
NM_001077183.3:c.1789C>T