Canonical Allele Identifier: PA2827483373
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1974289
ClinVar RCV Id: RCV002765551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336270.1:p.Ser447Leu
CA2491029
NM_001349341.3:c.1340C>T