Canonical Allele Identifier: PA2829971701
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65337

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Leu219Pro
CA022749
NM_021055.3:c.656T>C