Canonical Allele Identifier: PA2825574644
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 49751

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Leu826Pro
CA017496
NM_001114382.3:c.2477T>C