Canonical Allele Identifier: PA2825571699
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2981576
ClinVar RCV Id: RCV003840158

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107849.1:p.Leu211Arg
CA412951033
NM_001114377.2:c.632T>G
CA2740092151
NM_001114377.2:c.631_632delinsAG