Canonical Allele Identifier: PA2826066823
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3144202
ClinVar RCV Id: RCV004439075

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Ser359Leu
CA388884810
NM_001170629.2:c.1076C>T