Canonical Allele Identifier: PA2573066792
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1303798
ClinVar RCV Id: RCV001758091
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Pro386Gln
CA257556987
NM_001170629.2:c.1157C>A