Canonical Allele Identifier: PA645392486
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 383429
ClinVar RCV Id: RCV000437019 RCV000900269
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Glu146Gly
CA16607634
NM_005249.5:c.437A>G