Canonical Allele Identifier: PA915992122
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 300465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Asp702Asn
CA5546760
NM_001171934.1:c.2104G>A