Canonical Allele Identifier: PA2580319139
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1713694
ClinVar RCV Id: RCV002304289
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly131Ala
CA389475002
NM_005249.5:c.392G>C