Canonical Allele Identifier: PA137400
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45932
ClinVar RCV Id: RCV000039166 RCV001044674 RCV001105662 RCV001105663
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Val1299Ile
CA137399
NM_001171930.2:c.3895G>A