Canonical Allele Identifier: PA314587
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 205473
ClinVar RCV Id: RCV000187443 RCV000704363 RCV002317096
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Glu144Asp
CA314586
NM_005249.5:c.432G>C
CA389475081
NM_005249.5:c.432G>T