Canonical Allele Identifier: PA2829797385
Gene: CHD5 HGNC NCBI

Linked Data

ClinVar Variation Id: 3067854
ClinVar RCV Id: RCV003993542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056372.1:p.Asn1683His
CA338066829
NM_015557.3:c.5047A>C