Allele Registry

Canonical Allele Identifier: PA233248

Gene: FOXP1 HGNC NCBI

ClinVar RCV:

RCV000144697

ClinVar Variation:

156541

HGVS (amino-acid)	Matching Registered Transcripts
NP_116071.2:p.Trp534Arg	CA233247 NM_032682.6:c.1600T>C CA353491589 NM_032682.6:c.1600T>A