Canonical Allele Identifier: PA2573093229
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1313796
ClinVar RCV Id: RCV001769442 RCV001868608 RCV002489803
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Gln1599Glu
CA4760193
NM_017780.4:c.4795C>G