Canonical Allele Identifier: PA137586
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46042
ClinVar RCV Id: RCV000039278 RCV000086977 RCV000273869 RCV000331245 RCV001276795
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg3Cys
CA137585
NM_022124.6:c.7C>T