Canonical Allele Identifier: PA2826092937
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1376738
ClinVar RCV Id: RCV001912093

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Arg1215His
CA5544795
NM_001171930.2:c.3644G>A