Canonical Allele Identifier: PA093143
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 11407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054728.2:p.Arg397Trp
CA255855
NM_014009.4:c.1189C>T