Canonical Allele Identifier: PA2825571763
Gene: FOXP3 HGNC NCBI

Linked Data

ClinVar Variation Id: 373204
ClinVar RCV Id: RCV000414229
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001107849.1:p.Met335Val
CA16043289
NM_001114377.2:c.1003A>G