Canonical Allele Identifier: PA137383
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45923
ClinVar RCV Id: RCV000039156 RCV001105557 RCV000886092 RCV001106699 RCV001826570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val1192Ile
CA137382
NM_022124.6:c.3574G>A