Canonical Allele Identifier: PA2827484900
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336272.1:p.Ala311Thr
CA2491051
NM_001349343.3:c.931G>A