Canonical Allele Identifier: PA645420410
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 266127
ClinVar RCV Id: RCV000256716
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264.2:p.Arg1173Leu
CA10588999
NM_001273.5:c.3518G>T