Canonical Allele Identifier: PA2829936004
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2909677
ClinVar RCV Id: RCV003732380
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Ser110Asn
CA7091833
NM_020920.4:c.329G>A