Canonical Allele Identifier: PA2828421207
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65243

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.His1577Arg
CA021150
NM_001370405.1:c.4730A>G