Canonical Allele Identifier: PA199448
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 189623
ClinVar RCV Id: RCV000170086 RCV003235088
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Asn227Lys
CA199447
NM_005249.5:c.681C>G
CA389475640
NM_005249.5:c.681C>A