Canonical Allele Identifier: PA206113
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211032

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Glu144Lys
CA206112
NM_005249.5:c.430G>A