Canonical Allele Identifier: PA2829936513
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2875651
ClinVar RCV Id: RCV003707346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Asn1220Thr
CA388893718
NM_020920.4:c.3659A>C