Canonical Allele Identifier: PA2829936325
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2581900
ClinVar RCV Id: RCV003332606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Pro700Leu
CA388903684
NM_020920.4:c.2099C>T