Canonical Allele Identifier: PA199443
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 189619
ClinVar RCV Id: RCV000170081
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser234Pro
CA199442
NM_005249.5:c.700T>C