Canonical Allele Identifier: PA2826066813
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 930650

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Val344Met
CA7091857
NM_001170629.2:c.1030G>A