Canonical Allele Identifier: PA2826092029
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 446443
ClinVar RCV Id: RCV000515704
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Asp645Gly
CA377132590
NM_001171930.2:c.1934A>G