Canonical Allele Identifier: PA645392515
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 425040
ClinVar RCV Id: RCV000503039 RCV000487770 RCV002260643
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Amino-acid Alleles

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