Canonical Allele Identifier: PA137316
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg747Cys
CA137315
NM_022124.6:c.2239C>T