Canonical Allele Identifier: PA2826096022
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 422135

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165403.1:p.Asn206Thr
CA5543487
NM_001171932.2:c.617A>C