Allele Registry

Canonical Allele Identifier: PA2826092029

Gene: CDH23 HGNC NCBI

ClinVar Allele:

439911

ClinVar RCV:

RCV000515704

ClinVar Variation:

446443

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165401.1:p.Asp645Gly	CA377132590 NM_001171930.2:c.1934A>G