Canonical Allele Identifier: PA2741842023
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2909677
ClinVar RCV Id: RCV003732380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Ser389Asn
CA7091833
NM_001170629.2:c.1166G>A