Canonical Allele Identifier: PA2826095871
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165403.1:p.Val154Met
CA137437
NM_001171932.2:c.460G>A