Canonical Allele Identifier: PA2827484045
Gene: FOXP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2989815
ClinVar RCV Id: RCV003842446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001336271.1:p.Arg261Cys
CA2491106
NM_001349342.3:c.781C>T