Canonical Allele Identifier: PA2826841257
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 417890
ClinVar RCV Id: RCV000477959

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Tyr1242Asp
CA16616922
NM_001297553.2:c.3724T>G