Canonical Allele Identifier: PA645420453
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 421506
ClinVar RCV Id: RCV000481917 RCV002470871
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Ala922Thr
CA16619837
NM_001170629.2:c.2764G>A