Canonical Allele Identifier: PA2826066807
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 589689
ClinVar RCV Id: RCV001766584 RCV002316914
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Gln331Arg
CA388885219
NM_001170629.2:c.992A>G