Canonical Allele Identifier: PA1139752529
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 853882
ClinVar RCV Id: RCV001058790 RCV004545887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val1497Ala
CA5545073
NM_022124.6:c.4490T>C