Canonical Allele Identifier: PA2829936164
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1679265
ClinVar RCV Id: RCV002226862

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Val365Ala
CA388879203
NM_020920.4:c.1094T>C