Canonical Allele Identifier: PA2573248880
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1508433
ClinVar RCV Id: RCV002016101

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Asp143Glu
CA7140598
NM_005249.5:c.429C>G
CA389475075
NM_005249.5:c.429C>A