Canonical Allele Identifier: PA2825575131
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 238007

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gln1010Glu
CA044006
NM_001114382.3:c.3028C>G