Canonical Allele Identifier: PA2826067342
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1712053
ClinVar RCV Id: RCV002293771
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Gly1010Arg
CA388903202
NM_001170629.2:c.3028G>C
CA388903204
NM_001170629.2:c.3028G>A