Canonical Allele Identifier: PA915992771
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 650501
ClinVar RCV Id: RCV000805661
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Leu116Pro
CA389474908
NM_005249.5:c.347T>C