Canonical Allele Identifier: PA645498808
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 300459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp2667His
CA5546501
NM_022124.6:c.7999G>C