Canonical Allele Identifier: PA2826096158
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165403.1:p.Arg301Gln
CA239352
NM_001171932.2:c.902G>A