Canonical Allele Identifier: PA2826097191
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46048

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165404.1:p.Val563Ile
CA137596
NM_001171933.1:c.1687G>A