Canonical Allele Identifier: PA658830158
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 547390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Leu189Val
CA389475372
NM_005249.5:c.565C>G