Canonical Allele Identifier: PA2826957686
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 195324
ClinVar RCV Id: RCV000175886
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ser91Asn
CA241705
NM_001316690.1:c.272G>A