Canonical Allele Identifier: PA1139731884
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 854732

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054728.2:p.Arg358Gln
CA412948957
NM_014009.4:c.1073G>A