Canonical Allele Identifier: PA2827010942
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 535974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val290Ile
CA276776626
NM_001318829.2:c.868G>A