Canonical Allele Identifier: PA645498503
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 300441
ClinVar RCV Id: RCV000288653 RCV000594106 RCV001273555 RCV000343595 RCV003475927 RCV003165814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr1743Asn
CA5545691
NM_022124.6:c.5228C>A