Allele Registry

Canonical Allele Identifier: PA137398

Gene: CDH23 HGNC NCBI

ClinVar Allele:

55096

ClinVar RCV:

RCV000039165

RCV000950191

RCV001103711

RCV001103712

RCV001272567

RCV001797050

ClinVar Variation:

45931

HGVS (amino-acid)	Matching Registered Transcripts
NP_071407.4:p.Asn1282Ser	CA137396 NM_022124.6:c.3845A>G