Canonical Allele Identifier: PA2580319140
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716037
ClinVar RCV Id: RCV002295816

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly131Val
CA389475001
NM_005249.5:c.392G>T