Canonical Allele Identifier: PA645392471
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 380242
ClinVar RCV Id: RCV000585314 RCV001365335 RCV003448305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro84His
CA16606972
NM_005249.5:c.251C>A