Canonical Allele Identifier: PA658677763
Gene: FOXG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 487321
ClinVar RCV Id: RCV000576277 RCV001474993 RCV002315876
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005240.3:p.Pro79_Pro80dup
CA658658251
NM_005249.5:c.231_236dup
CA2590338731
NM_005249.5:c.235_240dup