Canonical Allele Identifier: PA172192
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 158598

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly252Val
CA172191
NM_005249.5:c.755G>T