Canonical Allele Identifier: PA2826841231
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3029660
ClinVar RCV Id: RCV003898920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Asn1127Ser
CA383582798
NM_001297553.2:c.3380A>G