Canonical Allele Identifier: PA2573281986
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1404452
ClinVar RCV Id: RCV001901651
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Leu1874Arg
CA5545818
NM_022124.6:c.5621T>G