Canonical Allele Identifier: PA2825440496
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001070651.1:p.Val825Leu
CA039144
NM_001077183.3:c.2473G>C