Canonical Allele Identifier: PA1139703501
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 839944
ClinVar RCV Id: RCV001041818
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Gly132Ser
CA389475003
NM_005249.5:c.394G>A