Allele Registry

Canonical Allele Identifier: PA2826335905

Gene: FOXP1 HGNC NCBI

ClinVar RCV:

RCV000144697

ClinVar Variation:

156541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001231742.1:p.Trp434Arg	CA233247 NM_001244813.1:c.1300T>C CA353491589 NM_001244813.1:c.1300T>A