Canonical Allele Identifier: PA2826841229
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 266126
ClinVar RCV Id: RCV000257626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Arg1120Gln
CA10588998
NM_001297553.2:c.3359G>A