Canonical Allele Identifier: PA891850254
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 579156
ClinVar RCV Id: RCV001401508
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser459Cys
CA389477130
NM_005249.5:c.1376C>G