Canonical Allele Identifier: PA2827019504
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2064694
ClinVar RCV Id: RCV002928875

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Lys1289Glu
CA394299259
NM_001318832.2:c.3865A>G