Canonical Allele Identifier: PA2829936008
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2836101
ClinVar RCV Id: RCV003689902
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Ser116Pro
CA388884445
NM_020920.4:c.346T>C