Allele Registry

Canonical Allele Identifier: PA645392515

Gene: FOXG1 HGNC NCBI

ClinVar Variation Id: 425040

HGVS (amino-acid)	Matching Registered Transcripts
NP_005240.3:p.Ile229Leu	CA16621657 NM_005249.5:c.685A>C