Allele Registry

Canonical Allele Identifier: PA094836

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000005371

ClinVar Variation:

5067

HGVS (amino-acid)	Matching Registered Transcripts
NP_055306.1:p.Arg553His	CA117244 NM_014491.4:c.1658G>A