Canonical Allele Identifier: PA645431861
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 405962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000539.2:p.Arg308Trp
CA056666
NM_000548.5:c.922C>T