Canonical Allele Identifier: PA2829983719
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066399.2:p.Arg1710Trp
CA054606
NM_021055.3:c.5128C>T