Canonical Allele Identifier: PA645392476
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 390253

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala90Ser
CA16607631
NM_005249.5:c.268G>T