Canonical Allele Identifier: PA2827013577
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305760.1:p.Val589Ile
CA038777
NM_001318831.2:c.1765G>A