Canonical Allele Identifier: PA137363
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45912
ClinVar RCV Id: RCV000039145 RCV000324074 RCV000376393 RCV001041387 RCV000764914 RCV001271862 RCV004528191
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val1088Met
CA137362
NM_022124.6:c.3262G>A