Canonical Allele Identifier: PA238811
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gln73Pro
CA238810
NM_005249.5:c.218A>C