Canonical Allele Identifier: PA2825573656
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val564Ile
CA032290
NM_001114382.3:c.1690G>A