Canonical Allele Identifier: PA2827009755
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 663392

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Gln1410Glu
CA394304316
NM_001318829.2:c.4228C>G