Canonical Allele Identifier: PA658667849
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 446446
ClinVar RCV Id: RCV000515743 RCV002251483 RCV003239292 RCV003476213
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg2029Trp
CA5545996
NM_022124.6:c.6085C>T