Canonical Allele Identifier: PA913194726
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 619984
ClinVar RCV Id: RCV000760184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264.2:p.Ile857Phe
CA383592115
NM_001273.5:c.2569A>T