Canonical Allele Identifier: PA2499270617
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1046219
ClinVar RCV Id: RCV001350744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Glu146del
CA7140599
NM_005249.5:c.436_438del