Canonical Allele Identifier: PA2828100041
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 266128
ClinVar RCV Id: RCV000257253
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350535.1:p.Trp1135Leu
CA10589000
NM_001363606.2:c.3404G>T