Canonical Allele Identifier: PA645420402
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 422274
ClinVar RCV Id: RCV000487222
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Lys399Gln
CA16619840
NM_001170629.2:c.1195A>C