Canonical Allele Identifier: PA2573248877
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406351
ClinVar RCV Id: RCV001935408
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ala121Pro
CA389474938
NM_005249.5:c.361G>C