Canonical Allele Identifier: PA2825572366
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1744511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Gln166Arg
CA276771986
NM_001114382.3:c.497A>G