Canonical Allele Identifier: PA2825439597
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Arg1686Trp
CA054606
NM_001077183.3:c.5056C>T