Canonical Allele Identifier: PA199439
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 189616
ClinVar RCV Id: RCV000170078 RCV000624178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala193Thr
CA199438
NM_005249.5:c.577G>A