Canonical Allele Identifier: PA2828416622
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Cys244Arg
CA022889
NM_001370405.1:c.730T>C