Canonical Allele Identifier: PA916050884
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 422135
ClinVar RCV Id: RCV000479707 RCV001828506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Asn206Thr
CA5543487
NM_052836.3:c.617A>C