Allele Registry

Canonical Allele Identifier: PA2826080650

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000234952

ClinVar Variation:

242975

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166237.1:p.Tyr530His	CA10584037 NM_001172766.3:c.1588T>C