Canonical Allele Identifier: PA2580155766
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1958787
ClinVar RCV Id: RCV002725640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Glu1771Val
CA388884037
NM_001170629.2:c.5312A>T