Canonical Allele Identifier: PA1139703483
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 936953
ClinVar RCV Id: RCV001205874
ClinVar Variation Id: 1201505
ClinVar RCV Id: RCV001566884
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly123Arg
CA7140595
NM_005249.5:c.367G>C
CA258396561
NM_005249.5:c.367G>A