Canonical Allele Identifier: PA915992169
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 226501

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Ala840Thr
CA5546937
NM_001171934.1:c.2518G>A