Canonical Allele Identifier: PA2573248878
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1522144
ClinVar RCV Id: RCV002028057

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly133Arg
CA389475009
NM_005249.5:c.397G>A
CA389475010
NM_005249.5:c.397G>C