Canonical Allele Identifier: PA915992068
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 522663

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Arg553Gln
CA5546637
NM_001171934.1:c.1658G>A