Canonical Allele Identifier: PA2829971326
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1744511

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Gln166Arg
CA276771986
NM_021055.3:c.497A>G