Canonical Allele Identifier: PA2826841186
Gene: CHD4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1301898
ClinVar RCV Id: RCV001733839
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001284482.1:p.Ser876Phe
CA383591496
NM_001297553.2:c.2627C>T