Canonical Allele Identifier: PA2826092901
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45923

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Val1192Ile
CA137382
NM_001171930.2:c.3574G>A