Canonical Allele Identifier: PA2580414187
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1754551
ClinVar RCV Id: RCV002364632
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu2210Gly
CA177354186
NM_017780.4:c.6629A>G