Canonical Allele Identifier: PA2825576215
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Glu1343Ala
CA050437
NM_001114382.3:c.4028A>C