Canonical Allele Identifier: PA2580319155
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1714370
ClinVar RCV Id: RCV002304352
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly141Val
CA389475062
NM_005249.5:c.422G>T