Canonical Allele Identifier: PA2827005286
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65146

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Met1588Thr
CA021670
NM_001318827.2:c.4763T>C