Canonical Allele Identifier: PA2826841175
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1710647
ClinVar RCV Id: RCV002291934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Phe814Val
CA383593084
NM_001297553.2:c.2440T>G