Canonical Allele Identifier: PA2827485725
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778
ClinVar RCV Id: RCV001926234 RCV002561328
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336273.1:p.Ala311Thr
CA2491051
NM_001349344.3:c.931G>A