Canonical Allele Identifier: PA314627
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205494
ClinVar RCV Id: RCV000187467

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala282Thr
CA314626
NM_005249.5:c.844G>A