Canonical Allele Identifier: PA2580170672
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_001264.2:p.Phe821Val
CA383593084
NM_001273.5:c.2461T>G