Canonical Allele Identifier: PA2826092771
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45912

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Val1088Met
CA137362
NM_001171930.2:c.3262G>A