Canonical Allele Identifier: PA891847637
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_065971.2:p.Gln52Arg
CA388885219
NM_020920.4:c.155A>G