Canonical Allele Identifier: PA357168
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 224139
ClinVar RCV Id: RCV000209877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Arg274Gln
CA357167
NM_005249.5:c.821G>A