Canonical Allele Identifier: PA2826093840
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Arg301Gln
CA239352
NM_001171931.2:c.902G>A