Canonical Allele Identifier: PA261802
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46040
ClinVar RCV Id: RCV000039276 RCV000725220 RCV000988383 RCV001264702 RCV001374881 RCV001559300 RCV004017329 RCV003473285 RCV003483451 RCV004528197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg2608His
CA261801
NM_022124.6:c.7823G>A