Canonical Allele Identifier: PA137318
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45891
ClinVar RCV Id: RCV000039124 RCV000487684 RCV000988379 RCV001034601 RCV001089680 RCV000787557 RCV001275939 RCV001331230 RCV001526743 RCV002477109
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.His755Tyr
CA137317
NM_022124.6:c.2263C>T