Canonical Allele Identifier: PA2828414633
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65229

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Val1456Met
CA020558
NM_001370404.1:c.4366G>A