Canonical Allele Identifier: PA2826092237
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Arg747Cys
CA137315
NM_001171930.2:c.2239C>T