Allele Registry

Canonical Allele Identifier: PA2827483528

Gene: FOXP1 HGNC NCBI

ClinVar RCV:

RCV000144697

ClinVar Variation:

156541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336270.1:p.Trp533Arg	CA233247 NM_001349341.3:c.1597T>C CA353491589 NM_001349341.3:c.1597T>A