Canonical Allele Identifier: PA2827484814
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 421700
ClinVar RCV Id: RCV000480408

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336272.1:p.Leu254Pro
CA16618010
NM_001349343.3:c.761T>C