Canonical Allele Identifier: PA2826094028
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Val424Met
CA5543746
NM_001171931.2:c.1270G>A