Canonical Allele Identifier: PA2580197646
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2494843
ClinVar RCV Id: RCV003216242
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala665Thr
CA4760954
NM_001316690.1:c.1993G>A