Canonical Allele Identifier: PA2827008406
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Arg952Lys
CA018596
NM_001318829.2:c.2855G>A