Canonical Allele Identifier: PA2828416824
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357334.1:p.Arg308Trp
CA056666
NM_001370405.1:c.922C>T