Canonical Allele Identifier: PA2826091257
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 420355

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Ile258Val
CA5543550
NM_001171930.2:c.772A>G