Canonical Allele Identifier: PA2826092427
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45898
ClinVar RCV Id: RCV000039131 RCV000294284 RCV000349179 RCV000887995 RCV001275943 RCV004534825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Val858Ile
CA137330
NM_001171930.2:c.2572G>A