Canonical Allele Identifier: PA913196876
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 623838
ClinVar RCV Id: RCV000761871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro134Ser
CA389475017
NM_005249.5:c.400C>T