Allele Registry

Canonical Allele Identifier: PA658831698

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000234952

ClinVar Variation:

242975

HGVS (amino-acid)	Matching Registered Transcripts
NP_055306.1:p.Tyr531His	CA10584037 NM_014491.4:c.1591T>C