Canonical Allele Identifier: PA2825574290
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Ile723Phe
CA10583306
NM_001114382.3:c.2167A>T