Canonical Allele Identifier: PA182069
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 178301
ClinVar RCV Id: RCV000155045 RCV001060903 RCV001831962 RCV002484934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val623Ile
CA182068
NM_022124.6:c.1867G>A