Canonical Allele Identifier: PA2829970521
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 991903
ClinVar RCV Id: RCV001280190 RCV002537882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asn221Thr
CA5543516
NM_022124.6:c.662A>C