Canonical Allele Identifier: PA238811
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193306
ClinVar RCV Id: RCV000173367 RCV000648323 RCV000724697 RCV002426828 RCV003448278
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gln73Pro
CA238810
NM_005249.5:c.218A>C