Canonical Allele Identifier: PA137430
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45947
ClinVar RCV Id: RCV000039181 RCV000764918 RCV001106861 RCV001106862 RCV001244548 RCV001273543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ala1464Val
CA137429
NM_022124.6:c.4391C>T