Canonical Allele Identifier: PA2826092752
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162905

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Pro1077Leu
CA175482
NM_001171930.2:c.3230C>T