Canonical Allele Identifier: PA2741919981
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2713048
ClinVar RCV Id: RCV003515739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly118Arg
CA389474918
NM_005249.5:c.352G>A
CA389474919
NM_005249.5:c.352G>C