Canonical Allele Identifier: PA2580155611
Gene: CHD8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1959867
ClinVar RCV Id: RCV002710473
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164100.1:p.Val396Leu
CA7091829
NM_001170629.2:c.1186G>C
CA7091830
NM_001170629.2:c.1186G>T