Canonical Allele Identifier: PA2825571777
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 11407

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107849.1:p.Arg362Trp
CA255855
NM_001114377.2:c.1084C>T