Canonical Allele Identifier: PA2573248876
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1626431
ClinVar RCV Id: RCV002110724
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala121Gly
CA389474941
NM_005249.5:c.362C>G