Canonical Allele Identifier: PA2827020999
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Arg1697Trp
CA054606
NM_001318832.2:c.5089C>T