Allele Registry

Canonical Allele Identifier: PA645420456

Gene: CHD8 HGNC NCBI

ClinVar RCV:

RCV000432820

ClinVar Variation:

390288

HGVS (amino-acid)	Matching Registered Transcripts
NP_001164100.1:p.Gly1322Arg	CA16607584 NM_001170629.2:c.3964G>C