Canonical Allele Identifier: PA2580319407
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1878746
ClinVar RCV Id: RCV002511247

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly481Arg
CA389477270
NM_005249.5:c.1441G>A
CA389477271
NM_005249.5:c.1441G>C