Canonical Allele Identifier: PA2825576461
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50125

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1419Lys
CA020286
NM_001114382.3:c.4255G>A