Canonical Allele Identifier: PA2573248879
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1509464
ClinVar RCV Id: RCV002017920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly135Val
CA389475026
NM_005249.5:c.404G>T