Canonical Allele Identifier: PA2828415555
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357333.1:p.Arg1701Cys
CA054522
NM_001370404.1:c.5101C>T