Canonical Allele Identifier: PA2826096906
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1677240
ClinVar RCV Id: RCV002223098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165404.1:p.Ile429Val
CA377162141
NM_001171933.1:c.1285A>G