Allele Registry

Canonical Allele Identifier: PA658831699

Gene: FOXP2 HGNC NCBI

ClinVar Allele:

244039

ClinVar RCV:

RCV000234955

ClinVar Variation:

242952

HGVS (amino-acid)	Matching Registered Transcripts
NP_055306.1:p.Asn597His	CA4446208 NM_014491.4:c.1789A>C