Canonical Allele Identifier: PA314603
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205481
ClinVar RCV Id: RCV000187452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala119Ser
CA314602
NM_005249.5:c.355G>T