Canonical Allele Identifier: PA2829593699
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3096392
ClinVar RCV Id: RCV004392262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Lys127Glu
CA389474972
NM_005249.5:c.379A>G