Canonical Allele Identifier: PA239353
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg301Gln
CA239352
NM_022124.6:c.902G>A