Canonical Allele Identifier: PA2826094322
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45879

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Arg546Gln
CA137295
NM_001171931.2:c.1637G>A