Allele Registry

Canonical Allele Identifier: PA645379683

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000234952

ClinVar Variation:

242975

HGVS (amino-acid)	Matching Registered Transcripts
NP_683696.2:p.Tyr556His	CA10584037 NM_148898.4:c.1666T>C