Canonical Allele Identifier: PA1139703330
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 954627
ClinVar RCV Id: RCV001227120
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro85Ser
CA389474721
NM_005249.5:c.253C>T