Canonical Allele Identifier: PA2741919980
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2878727
ClinVar RCV Id: RCV003628812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Asp117Gly
CA389474915
NM_005249.5:c.350A>G