Canonical Allele Identifier: PA2827019510
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Leu1291Pro
CA394299288
NM_001318832.2:c.3872T>C