Canonical Allele Identifier: PA2826094980
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Val858Ile
CA137330
NM_001171931.2:c.2572G>A