Allele Registry

Canonical Allele Identifier: PA915992017

Gene: CDH23 HGNC NCBI

ClinVar Allele:

407904

ClinVar RCV:

RCV000485626

RCV000507978

RCV001089682

RCV001839003

ClinVar Variation:

422345

HGVS (amino-acid)	Matching Registered Transcripts
NP_001165405.1:p.Asp455Asn	CA5546544 NM_001171934.1:c.1363G>A