Canonical Allele Identifier: PA2829936506
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1805482
ClinVar RCV Id: RCV002471900
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Cys1204Ser
CA388894019
NM_020920.4:c.3611G>C
CA388894029
NM_020920.4:c.3610T>A