Allele Registry

Canonical Allele Identifier: PA915992197

Gene: CDH23 HGNC NCBI

ClinVar RCV:

RCV000504591

ClinVar Variation:

437904

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165405.1:p.Arg898Trp	CA377136447 NM_001171934.1:c.2692C>T