Canonical Allele Identifier: PA2829936900
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1254644
ClinVar RCV Id: RCV001658826 RCV003486998
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Ser1815del