Canonical Allele Identifier: PA2825437118
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 386865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Met986Val
CA044156
NM_001077183.3:c.2956A>G