Canonical Allele Identifier: PA2825573154
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu410Arg
CA014118
NM_001114382.3:c.1229T>G