Canonical Allele Identifier: PA314579
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205469
ClinVar RCV Id: RCV000187439 RCV000648322 RCV001704984 RCV002311266
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro82Gln
CA314578
NM_005249.5:c.245C>A