Canonical Allele Identifier: PA2741919952
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3042410
ClinVar RCV Id: RCV003924539
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro69del
CA7140590
NM_005249.5:c.206_208del