Canonical Allele Identifier: PA2827480455
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336266.2:p.Ala463Thr
CA2490866
NM_001349337.2:c.1387G>A