Canonical Allele Identifier: PA2827009367
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 207683

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1294Gln
CA050701
NM_001318829.2:c.3881G>A