Canonical Allele Identifier: PA2580197655
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1700819
ClinVar RCV Id: RCV002276287
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Asn693Ser
CA371307811
NM_001316690.1:c.2078A>G