Canonical Allele Identifier: PA2827011423
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 230946

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305758.1:p.Val740Ile
CA038777
NM_001318829.2:c.2218G>A