Canonical Allele Identifier: PA2827485820
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_001336273.1:p.Ala349Thr
CA353493393
NM_001349344.3:c.1045G>A