Canonical Allele Identifier: PA2825576675
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1477Met
CA020558
NM_001114382.3:c.4429G>A