Canonical Allele Identifier: PA2826092902
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 504469
ClinVar RCV Id: RCV000599331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Val1192Gly
CA377153098
NM_001171930.2:c.3575T>G
CA658797436
NM_001171930.2:c.3575_3576delinsGT