Canonical Allele Identifier: PA645392473
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 387087
ClinVar RCV Id: RCV000436439 RCV002059728
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gln86Glu
CA16607629
NM_005249.5:c.256C>G