Canonical Allele Identifier: PA2827005543
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305756.1:p.Arg1650Trp
CA054606
NM_001318827.2:c.4948C>T