Canonical Allele Identifier: PA915992816
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 807103
ClinVar RCV Id: RCV000995164
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ile211Asn
CA389475524
NM_005249.5:c.632T>A