Canonical Allele Identifier: PA314639
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205501
ClinVar RCV Id: RCV000187477 RCV001857611
ClinVar Variation Id: 1305522
ClinVar RCV Id: RCV001768729 RCV002077188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro111_Pro112dup
CA314638
NM_005249.5:c.327_332dup