Canonical Allele Identifier: PA2826957573
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1342438
ClinVar RCV Id: RCV001839189
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Gln526Arg
CA371303532
NM_001316690.1:c.1577A>G