Canonical Allele Identifier: PA2573248873
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1436807
ClinVar RCV Id: RCV001955342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro99Ala
CA389474806
NM_005249.5:c.295C>G