Canonical Allele Identifier: PA2826066826
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 3023811
ClinVar RCV Id: RCV003880906

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Pro364Ser
CA388884756
NM_001170629.2:c.1090C>T