Canonical Allele Identifier: PA2741964459
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3013617
ClinVar RCV Id: RCV003873192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ile2572Val
CA4760870
NM_017780.4:c.7714A>G