Canonical Allele Identifier: PA2499270616
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1213248
ClinVar RCV Id: RCV001589836

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro134Arg
CA389475019
NM_005249.5:c.401C>G