Canonical Allele Identifier: PA2826841177
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1308040
ClinVar RCV Id: RCV001773951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Arg829Cys
CA232392976
NM_001297553.2:c.2485C>T