Canonical Allele Identifier: PA2825311035
Gene: FOXP4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1472670
ClinVar RCV Id: RCV002286435 RCV001969335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001012427.1:p.Ala512Thr
CA364069908
NM_001012427.2:c.1534G>A