Canonical Allele Identifier: PA2826333933
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 391588

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001231737.1:p.Phe501Leu
CA16604636
NM_001244808.3:c.1503C>G
CA353492743
NM_001244808.3:c.1503C>A
CA353492756
NM_001244808.3:c.1501T>C