Canonical Allele Identifier: PA645392477
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 377165
ClinVar RCV Id: RCV000429748 RCV000685886 RCV003448303
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala92Val
CA16603285
NM_005249.5:c.275C>T