Canonical Allele Identifier: PA2826335652
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2989815
ClinVar RCV Id: RCV003842446
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231742.1:p.Arg261Cys
CA2491106
NM_001244813.1:c.781C>T