Canonical Allele Identifier: PA2827010433
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg1630Cys
CA054522
NM_001318829.2:c.4888C>T