Canonical Allele Identifier: PA234035
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 167092
ClinVar RCV Id: RCV000153265 RCV000500932 RCV002260625
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly224Ser
CA234034
NM_005249.5:c.670G>A