Canonical Allele Identifier: PA658807300
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 545092
ClinVar RCV Id: RCV000656311 RCV003448331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Leu257Pro
CA389475835
NM_005249.5:c.770T>C