Allele Registry

Canonical Allele Identifier: PA2830289490

Gene: FOXP2 HGNC NCBI

ClinVar RCV:

RCV000234952

ClinVar Variation:

242975

HGVS (amino-acid)	Matching Registered Transcripts
NP_683698.2:p.Tyr548His	CA10584037 NM_148900.4:c.1642T>C