Canonical Allele Identifier: PA2829936166
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2258787
ClinVar RCV Id: RCV002772973

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Arg372Gln
CA388879116
NM_020920.4:c.1115G>A