Canonical Allele Identifier: PA2827003024
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 229369

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Gly921Glu
CA043736
NM_001318827.2:c.2762G>A