Canonical Allele Identifier: PA2827010905
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 468193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val270Met
CA394315689
NM_001318829.2:c.808G>A