Canonical Allele Identifier: PA2827484298
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336271.1:p.Phe402Leu
CA16604636
NM_001349342.3:c.1206C>G
CA353492743
NM_001349342.3:c.1206C>A
CA353492756
NM_001349342.3:c.1204T>C