Canonical Allele Identifier: PA891850200
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 572556
ClinVar RCV Id: RCV000693965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly148Asp
CA389475107
NM_005249.5:c.443G>A