Canonical Allele Identifier: PA2825571760
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 11419
ClinVar RCV Id: RCV000012172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107849.1:p.Phe332Leu
CA255875
NM_001114377.2:c.994T>C
CA329133742
NM_001114377.2:c.996C>G
CA412948816
NM_001114377.2:c.996C>A