Canonical Allele Identifier: PA2741842258
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2992652
ClinVar RCV Id: RCV003857763

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Glu2097Gln
CA7090808
NM_001170629.2:c.6289G>C