Canonical Allele Identifier: PA2826334514
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231739.1:p.Ala580Thr
CA2490866
NM_001244810.1:c.1738G>A