Canonical Allele Identifier: PA645392499
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 369885
ClinVar RCV Id: RCV000408825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Ser185Ile
CA10654909
NM_005249.5:c.554G>T