Allele Registry

Canonical Allele Identifier: PA2826092812

Gene: CDH23 HGNC NCBI

ClinVar Allele:

55082

ClinVar RCV:

RCV000039150

RCV000965142

RCV001103613

RCV001103614

RCV001831660

ClinVar Variation:

45917

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165401.1:p.Leu1122Val	CA137372 NM_001171930.2:c.3364T>G