Canonical Allele Identifier: PA2825574596
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 467942

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107854.1:p.Val813Met
CA039041
NM_001114382.3:c.2437G>A