Canonical Allele Identifier: PA2827483567
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336270.1:p.Ala563Thr
CA2490866
NM_001349341.3:c.1687G>A