Canonical Allele Identifier: PA253329
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp2202Asn
CA253328
NM_022124.6:c.6604G>A