Canonical Allele Identifier: PA2573068908
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1333566

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264.2:p.Arg813His
CA383593243
NM_001273.5:c.2438G>A