Canonical Allele Identifier: PA2829935999
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_065971.2:p.Pro107Gln
CA257556987
NM_020920.4:c.320C>A