Canonical Allele Identifier: PA2741846312
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3029660
ClinVar RCV Id: RCV003898920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001264.2:p.Asn1134Ser
CA383582798
NM_001273.5:c.3401A>G