Allele Registry

Canonical Allele Identifier: PA645379690

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000234955

ClinVar Variation:

242952

HGVS (amino-acid)	Matching Registered Transcripts
NP_683696.2:p.Asn622His	CA4446208 NM_148898.4:c.1864A>C