Canonical Allele Identifier: PA2826096046
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 991903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165403.1:p.Asn221Thr
CA5543516
NM_001171932.2:c.662A>C