Canonical Allele Identifier: PA2829980741
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1366Gln
CA050701
NM_021055.3:c.4097G>A