Canonical Allele Identifier: PA2826957572
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2198012
ClinVar RCV Id: RCV002629060
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.His524Tyr
CA4759517
NM_001316690.1:c.1570C>T