Canonical Allele Identifier: PA314634
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205498
ClinVar RCV Id: RCV000187472

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser459Ala
CA314633
NM_005249.5:c.1375T>G