Canonical Allele Identifier: PA2828418295
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 237983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Ile723Val
CA10583305
NM_001370405.1:c.2167A>G