Canonical Allele Identifier: PA658807288
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 538816
ClinVar RCV Id: RCV000648315

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Asn232Asp
CA389475664
NM_005249.5:c.694A>G