Allele Registry

Canonical Allele Identifier: PA2830289494

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000005371

ClinVar Variation:

5067

HGVS (amino-acid)	Matching Registered Transcripts
NP_683698.2:p.Arg570His	CA117244 NM_148900.4:c.1709G>A