Allele Registry

Canonical Allele Identifier: PA916078523

Gene: FOXP2 HGNC NCBI

ClinVar Allele:

192457

ClinVar RCV:

RCV000175859

RCV000234933

RCV002336427

RCV003927612

ClinVar Variation:

195296

HGVS (amino-acid)	Matching Registered Transcripts
NP_683698.2:p.Gln17Leu	CA241662 NM_148900.4:c.50A>T