Canonical Allele Identifier: PA2829936908
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2992652
ClinVar RCV Id: RCV003857763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Glu1818Gln
CA7090808
NM_020920.4:c.5452G>C