Canonical Allele Identifier: PA093156
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 11409
ClinVar RCV Id: RCV000012162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_054728.2:p.Phe371Cys
CA255857
NM_014009.4:c.1112T>G