Allele Registry

Canonical Allele Identifier: PA2826080677

Gene: FOXP2 HGNC NCBI

ClinVar Allele:

244039

ClinVar RCV:

RCV000234955

ClinVar Variation:

242952

HGVS (amino-acid)	Matching Registered Transcripts
NP_001166237.1:p.Asn596His	CA4446208 NM_001172766.3:c.1786A>C