Canonical Allele Identifier: PA2825577298
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 65153

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val1650Phe
CA021508
NM_001114382.3:c.4948G>T