Allele Registry

Canonical Allele Identifier: PA2826336751

Gene: FOXP1 HGNC NCBI

ClinVar Allele:

70500

ClinVar RCV:

RCV000049262

RCV000049263

RCV000175486

RCV000437146

RCV002311531

RCV003934994

ClinVar Variation:

55847

HGVS (amino-acid)	Matching Registered Transcripts
NP_001231743.1:p.Pro568Ser	CA201483 NM_001244814.1:c.1702C>T