Canonical Allele Identifier: PA182076
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 178305
ClinVar RCV Id: RCV000155049 RCV000279211 RCV000338894 RCV000900747 RCV001291212 RCV004528887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ala1631Val
CA182075
NM_022124.6:c.4892C>T