Canonical Allele Identifier: PA2826841236
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 266128
ClinVar RCV Id: RCV000257253
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Trp1141Leu
CA10589000
NM_001297553.2:c.3422G>T