Canonical Allele Identifier: PA314565
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205462

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.His55_His57del
CA314564
NM_005249.5:c.153_161del
CA2125998747
NM_005249.5:c.162_170del