Canonical Allele Identifier: PA2825436230
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50106

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Cys696Tyr
CA016643
NM_001077183.3:c.2087G>A