Allele Registry

Canonical Allele Identifier: PA2827485158

Gene: FOXP1 HGNC NCBI

ClinVar RCV:

RCV000144697

ClinVar Variation:

156541

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336272.1:p.Trp433Arg	CA233247 NM_001349343.3:c.1297T>C CA353491589 NM_001349343.3:c.1297T>A