Canonical Allele Identifier: PA2826841173
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Arg806His
CA383593243
NM_001297553.2:c.2417G>A