Canonical Allele Identifier: PA2825574572
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49725

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Cys804Arg
CA017384
NM_001114382.3:c.2410T>C