Canonical Allele Identifier: PA2827002843
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1516394

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Pro866Thr
CA394279461
NM_001318827.2:c.2596C>A