Canonical Allele Identifier: PA2741842024
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_001164100.1:p.Ser395Pro
CA388884445
NM_001170629.2:c.1183T>C