Canonical Allele Identifier: PA2826338188
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 451160
ClinVar RCV Id: RCV000523347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231745.1:p.Ala450Thr
CA353493393
NM_001244816.1:c.1348G>A