Allele Registry

Canonical Allele Identifier: PA2830289522

Gene: FOXP2 HGNC NCBI

ClinVar Allele:

244039

ClinVar RCV:

RCV000234955

ClinVar Variation:

242952

HGVS (amino-acid)	Matching Registered Transcripts
NP_683698.2:p.Asn614His	CA4446208 NM_148900.4:c.1840A>C