Canonical Allele Identifier: PA2580449771
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2153297
ClinVar RCV Id: RCV003077538
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ile2118Val
CA377154498
NM_022124.6:c.6352A>G