Canonical Allele Identifier: PA2580319403
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2003976
ClinVar RCV Id: RCV002828143

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Thr476Ala
CA389477234
NM_005249.5:c.1426A>G