Canonical Allele Identifier: PA2827483283
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1422778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336270.1:p.Ala411Thr
CA2491051
NM_001349341.3:c.1231G>A