Canonical Allele Identifier: PA2827003284
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Val1022Met
CA045672
NM_001318827.2:c.3064G>A