Canonical Allele Identifier: PA2828420232
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064694
ClinVar RCV Id: RCV002928875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Lys1302Glu
CA394299259
NM_001370405.1:c.3904A>G