Canonical Allele Identifier: PA2829970839
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1006937

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val424Met
CA5543746
NM_022124.6:c.1270G>A