Canonical Allele Identifier: PA2828099982
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308040
ClinVar RCV Id: RCV001773951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350535.1:p.Arg823Cys
CA232392976
NM_001363606.2:c.2467C>T