Canonical Allele Identifier: PA100996
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 189620
ClinVar RCV Id: RCV000170082
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Arg244Cys
CA199444
NM_005249.5:c.730C>T