Canonical Allele Identifier: PA2827002332
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 536065

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg712Trp
CA037721
NM_001318827.2:c.2134C>T