Canonical Allele Identifier: PA2580414007
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1800792
ClinVar RCV Id: RCV002462389
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Pro1556Ala
CA371318958
NM_017780.4:c.4666C>G