Canonical Allele Identifier: PA2828421694
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535984

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg1702Gln
CA394314713
NM_001370405.1:c.5105G>A