Canonical Allele Identifier: PA2827485692
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2635630
ClinVar RCV Id: RCV003427949 RCV003732578
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336273.1:p.Thr289Ser
CA2491064
NM_001349344.3:c.866C>G
CA2491065
NM_001349344.3:c.865A>T