Canonical Allele Identifier: PA2580155632
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2258787
ClinVar RCV Id: RCV002772973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Arg651Gln
CA388879116
NM_001170629.2:c.1952G>A