Canonical Allele Identifier: PA2826335930
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2441549

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231742.1:p.Ala464Thr
CA2490866
NM_001244813.1:c.1390G>A