Canonical Allele Identifier: PA2741842130
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 2581900
ClinVar RCV Id: RCV003332606

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Pro979Leu
CA388903684
NM_001170629.2:c.2936C>T