Allele Registry

Canonical Allele Identifier: PA2826080657

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000005371

ClinVar Variation:

5067

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166237.1:p.Arg552His	CA117244 NM_001172766.3:c.1655G>A