Canonical Allele Identifier: PA2826096048
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016579
ClinVar RCV Id: RCV001315602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165403.1:p.Ile224Val
CA377112782
NM_001171932.2:c.670A>G