Canonical Allele Identifier: PA2827485043
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280463
ClinVar RCV Id: RCV000283441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336272.1:p.Tyr369Cys
CA2490997
NM_001349343.3:c.1106A>G