Canonical Allele Identifier: PA645392521
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 435240
ClinVar RCV Id: RCV000504441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Cys238Tyr
CA389475703
NM_005249.5:c.713G>A