Canonical Allele Identifier: PA2829981817
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1000977
ClinVar RCV Id: RCV001297190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Val1507Phe
CA394305002
NM_021055.3:c.4519G>T