Canonical Allele Identifier: PA2827019579
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Glu1310Ala
CA050437
NM_001318832.2:c.3929A>C