Canonical Allele Identifier: PA2499270618
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1024440
ClinVar RCV Id: RCV001324620 RCV003166900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly148Val
CA7140601
NM_005249.5:c.443G>T