Canonical Allele Identifier: PA2741977763
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3023811
ClinVar RCV Id: RCV003880906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065971.2:p.Pro85Ser
CA388884756
NM_020920.4:c.253C>T