Canonical Allele Identifier: PA2741919986
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2757001
ClinVar RCV Id: RCV003515153
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro142Ala
CA389475064
NM_005249.5:c.424C>G