Canonical Allele Identifier: PA172188
Gene: FOXG1 HGNC NCBI
ClinVar RCV:
RCV000145992
ClinVar Variation:
158596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala188Gly
CA172187
NM_005249.5:c.563C>G