Canonical Allele Identifier: PA2826067384
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 422245
ClinVar RCV Id: RCV000484621 RCV000709955 RCV001265457 RCV004551589
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Gly1103Val
CA16619836
NM_001170629.2:c.3308G>T