Canonical Allele Identifier: PA916050858
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Val154Met
CA137437
NM_052836.3:c.460G>A