Canonical Allele Identifier: PA208364
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 211031
ClinVar RCV Id: RCV000194286 RCV002054265 RCV003422095
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser462Gly
CA208363
NM_005249.5:c.1384A>G