Canonical Allele Identifier: PA2825576348
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406016

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1384Met
CA050677
NM_001114382.3:c.4150G>A