Canonical Allele Identifier: PA294777
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 158591
ClinVar RCV Id: RCV000145985 RCV000576256 RCV002316930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gln70Pro
CA294776
NM_005249.5:c.209A>C